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HRID 1769110Erstellt: 25. Oktober 2026

Potassium Chloride → 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione

https://huagongshe.com/reaction/1769110

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium ChlorideHCID 4873—
EduktCarbon DisulfideHCID 6348—
EduktPotassium AcetateHCID 517044—
EduktCarbamodithioic acidHCID 3001860—
Edukt2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochlorideHCID 19957059—
LösungsmittelIsopropanolHCID 3776—
Produkt1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 1497830738%

Reaktionsschritte

To a suspension of 15 g (50 mmol) of 2-[(methylamino)methyl]-α-phenylbenzenemethanamine dihydrochloride in 100 mL of isopropyl alcohol was added 10 g (100 mmol) of potassium acetate followed by 3.3 mL (55 mmol) of carbon disulfide in 35 mL of isopropyl alcohol. The suspension was stirred at room temperature for one and one-half hours and then refluxed for 30 minutes. The reaction was chilled in ice and the internal salt of the carbamodithioic acid, contaminated with two equivalents of potassium chloride, was filtered off. The carbamodithioic acid was suspended in 125 mL of 95% ethanol, and 1.3 mL of 12N hydrochloric acid was added. The suspension was refluxed for three days, cooled, and 15.3 g (114%) of the crude benzodiazepin-3-thione was filtered off. A 6-g portion of the crude product was recrystallized from 2-ethoxy ethanol to yield 2.0 g (38%) of product, mp 208-209.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05380721
Quelldatensatzuspto-grants-1995_01
ORD IDord-f0ac08a8be49426cafff99098869b47e
Quellennotizuspto-grants-1995_01